| ²é¿´: 196 | »Ø¸´: 1 | ||
shooter652Ìú³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
20.11,20.32,21.30,21.84,23.21,23.49,25.34,25.57,26.86,26.90,26.96,27.11,35.22,36.02,38.11,38.30,41.78,44.78,44.84,52.05,52.06,72.41,72.69,75.48,76.05,124.94,125.32,146.51 Ê®·Ö¸Ðл¡£ |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
353Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
²ÄÁϹ¤³Ì302·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çó
ÒѾÓÐ3È˻ظ´
²ÄÁÏÓ뻯¹¤363ÇóÍÆ¼ö
ÒѾÓÐ4È˻ظ´
085602µ÷¼Á ³õÊÔ×Ü·Ö335
ÒѾÓÐ11È˻ظ´
081700ѧ˶£¬323·Ö£¬Ò»Ö¾Ô¸Öйúº£Ñó´óѧÇóµ÷¼ÁѧУ
ÒѾÓÐ12È˻ظ´
085410È˹¤ÖÇÄÜ ³õÊÔ316·Ö Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
²ÄÁÏ»¯¹¤306·ÖÕÒºÏÊʵ÷¼Á
ÒѾÓÐ11È˻ظ´
Ц¶à»á»³ÔÐ
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1216 (½²Ê¦)
- ½ð±Ò: 9788.1
- É¢½ð: 610
- ºì»¨: 40
- ɳ·¢: 3
- Ìû×Ó: 2723
- ÔÚÏß: 1284.6Сʱ
- ³æºÅ: 2010893
- ×¢²á: 2012-09-18
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
shooter652: ½ð±Ò+8, ¡ïÓаïÖú 2014-05-26 19:01:01
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
shooter652: ½ð±Ò+8, ¡ïÓаïÖú 2014-05-26 19:01:01
|
²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½1153¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (20R,22R)-20,22,25-trihydroxy-2 ¦Â,3 ¦Â-(isopropylidenedioxy)-5¦Â-cholest-8(14)-en-6-one ÏàËÆ¶È:66.6% Russian Journal of Organic Chemistry 2010 46 1735-1740 ¦¤8(14)-14¦Á-deoxy- and 14¦Á-deoxy-14¦Á-hydroperoxyecdysteroids A. Sh. Ibragimova, N. A. Ves¡¯kina, I. V. Galyautdinov and V. N. Odinokov Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . cumingianol A C32H54O6 ÏàËÆ¶È:65.6% Phytochemistry 2011 72 2205-2211 Triterpenes and a triterpene glucoside from Dysoxylum cumingianum Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Á,12¦Á,16¦Â-Trihydroxy-5¦Â-cholan-24-oic acid C24H40O5 ÏàËÆ¶È:64.2% Steroids 2010 75 506-512 Synthesis, aggregation behavior and cholesterol solubilization studies of 16-epi-pythocholic acid (3¦Á,12¦Á,16¦Â-trihydroxy-5¦Â-cholan-24-oic acid) Nonappa, Uday Maitra Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3,20,24,25-tetrahydroxydammarane C30H54O4 ÏàËÆ¶È:63.3% Phytochemistry 2004 65 2173-2176 Insect antifeedant compounds from Nothofagus dombeyi and N. pumilio Odile Thoison, Thierry S¨¦venet, Hermann M. Niemeyer, Graeme B. Russell Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . panicualtin D C32H52O7 ÏàËÆ¶È:63.3% Journal of the Indian Chemical Society 1999 76 575-581 Study of the stereochemistry of new tetranortriterpenoids isolated from root-wood of Chisocheton paniculatus Hiern(Meliaceae) R.D.Yadav,J.C.S.Kataky and R.K.Mathur Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Cumingianol B C32H54O6 ÏàËÆ¶È:62.5% Phytochemistry 2011 72 2205-2211 Triterpenes and a triterpene glucoside from Dysoxylum cumingianum Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Cumingianol C C32H52O5 ÏàËÆ¶È:62.5% Phytochemistry 2011 72 2205-2211 Triterpenes and a triterpene glucoside from Dysoxylum cumingianum Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . paniculatin-D C32H52O7 ÏàËÆ¶È:62.5% Indian Journal of Chemistry Section B 1999 38B 1359-1363 New protolimonoids and limonoids art I-isolation,structure elucidation of new protolimonoids and limonoid from the root wood of Chisocheton paniculatus Hiern(Meliaceae)R D Yadav, J C S Kataky&R K mathur Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Kadpolysperin C C32H50O5 ÏàËÆ¶È:62.5% Tetrahedron 2012 68 4820-4829 Kadpolysperins A¨CN, lanostane triterpene acids possessing rich structure types from Kadsura polysperma Ke Dong, Jian-Xin Pu, Xue Du, Jia Su, Xiao-Nian Li, Jian-Hong Yang, Wei Zhao, Yan Li, Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-05-26 09:29:36














»Ø¸´´ËÂ¥
art I-isolation,structure elucidation of new protolimonoids and limonoid from the root wood of Chisocheton paniculatus Hiern(Meliaceae)